A pump system is disclosed that comprises a control unit and one or more modular pumping units removably docked to the primary control unit. Each modular pumping unit comprises a pumping mechanism and a processor configured to control the pumping mechanism and communicate with the control unit. The modular pumping unit is configured to manipulate a portion of a fluid delivery set to pump a fluid. The first processor and the second processor are configured to exchange one or more operating parameters when the modular pumping unit is docked to the primary control unit. The modular pumping unit is configured to pump the fluid after being undocked.

The present disclosure describes a system and method for varying pressure from a pressure generator without pressure generator motor speed variations. The system comprises a pressure generator housing, a centrifugal compressor housed within the housing, and at least one impeller blade. The centrifugal compressor is configured to generate a pressurized flow of gas. The pressure generator system includes a pressure adjustment body (e.g., a plate) that is movably attached to and/or within the housing, and an actuator configured to displace the pressure adjustment body with respect to the housing, such that displacement of the pressure adjustment body is configured to regulate pressure of the generated gas flow by varying a gap between the impeller blade and a surface of the pressure adjustment body.

The application discloses a noise attenuating system (100, 200, 300, 400, 700, 800) for use with a positive airway pressure system providing a flow of gas, comprising: an expansion chamber (140, 240, 340, 434, 740) having a volume; an intake tube (115, 215, 315, 415, 715, 815) having an inlet (117, 217, 317, 410, 717, 812) and outlet port or portion separated by a length, wherein a portion of the inlet port or portion extends outside of the expansion chamber; and either: a noise attenuator (110, 120, 170, 210, 220, 223, 224, 226, 228, 232, 270, 320, 411, 413, 422, 423, 424, 425, 426, 428, 431, 720, 722) having a bottom and protruding sidewall forming a cavity, wherein the noise attenuator is positioned near the inlet portion of the intake tube such that a portion of the intake tube extends into the cavity of the noise attenuator; or: an acoustic deflector (110, 120, 170, 210, 220, 223, 224, 226, 228, 270, 232, 320, 411, 413, 422, 423, 424, 425, 426, 428, 431, 720, 722) positioned near the outlet port or portion of the intake tube, wherein noise is deflected away from the outlet port or portion of the intake tube. The application also discloses positive air pressure apparatus (100, 200, 300, 400, 700, 800) comprising a housing (180, 480, 880, 884), first and second acoustic chambers, an intake vent or port (125, 225, 410, 812) in the first chamber, an inlet port or tube coupling the first and second chambers, a noise attenuator in the first chamber, and a blower unit (150, 250, 350, 440) in the second chamber.

An automated peritoneal dialysis system provides both cycler-assisted peritoneal dialysis treatment and also continuous ambulatory peritoneal dialysis (CAPD). The system includes a fluid preparation and treatment device with a concentrate dilution components connected to a source of purified water and medicament concentrate. The treatment device has at least one mixing container connected via a pump and valves to the sources, the valves and the pump mixing and diluting the concentrate to form a medicament. An auxiliary port is provided for attaching a CAPD container and for receiving medicament. A controller is programmed to control the fluid preparation and treatment device to implement one or more cycler-assisted peritoneal dialysis treatment cycles using medicament from the mixing container and also to control the preparation of additional dialysate at the end of the cycler-assisted peritoneal dialysis treatment cycles to dispense additional dialysate through the auxiliary port for use in CAPD.

A treatment device system includes a treatment machine for performing a therapy on a patient, the treatment machine including at least one fluid conveyor and a controller, the controller having a first memory, to cause the at least one fluid conveyor to produce a therapeutic fluid by mixing purified water and at least one concentrate. The system also includes and a water purifier in fluid communication with and providing the purified water to the treatment machine. A wired or wireless control line provides two way communication between the controller of the treatment machine and the internal central controller of the water purifier, wherein the controller of the treatment machine transmits data via the control line to the internal central controller of the water purifier for control of the water purifier, the data provided based on at least one of the operator inputs received via the user interface.

A treatment device system includes a treatment machine for performing a therapy on a patient, the treatment machine including at least one fluid conveyor and a controller, the controller having a first memory, to cause the at least one fluid conveyor to produce a therapeutic fluid by mixing purified water and at least one concentrate. The system also includes and a water purifier in fluid communication with and providing the purified water to the treatment machine. A wired or wireless control line provides two way communication between the controller of the treatment machine and the internal central controller of the water purifier, wherein the controller of the treatment machine transmits data via the control line to the internal central controller of the water purifier for control of the water purifier, the data provided based on at least one of the operator inputs received via the user interface.

Systems and methods are provided to limit abdominal distension and alleviate uncomfortable side effects related to it—in patients treated in hydrocolonic preparation units. Systems may comprise a water delivery unit comprising a controllable water supply, configured to introduce water controllably into the patient's large intestine, a drainage configured to drain, by gravity, the introduced water with contents of the patient's large intestine and a controller. The drainage comprises a drainage pipe and sensor(s) such as camera(s) configured to continuously measure the amount of drained water drained by the drainage pipe. The controller is configured to control the water introduction with respect to the measured amount of drained water, keeping an amount of water retained in the patient below a specified water retention threshold to reduce uncomfortable side effects of abdominal distension.

A waste collection unit for collecting waste material. First and second waste containers are supported on a portable cart. A control panel is configured to receive one or more inputs of selectively set vacuum levels in the first and/or second waste containers. A control system controls operation of vacuum regulators based on the input(s) to regulate levels of vacuums being drawn in each of the waste containers. Pressure sensors in communication with the control system may be positioned to monitor pressure in the waste containers. A back up port support on the portable cart may be provided to receive a vacuum line for coupling a vacuum manifold to a remote vacuum source not located on the portable cart. Container lamps may be coupled to the first and/or second waste containers and configured to illuminate the waste material within the waste containers to be viewed through transparent windows.

An infusion system for being operatively connected to a fluid delivery line and to an infusion container includes a pump, a plurality of different types of sensors connected to the pump or the fluid delivery line, at least one processor, and a memory. The plurality of different types of sensors are configured to indicate whether air is in the fluid delivery line. The memory includes programming code for execution by the at least one processor. The programming code is configured to, based on measurements taken by the plurality of different types of sensors, determine: whether there is air in the fluid delivery line; whether there is a partial occlusion or a total occlusion in the fluid delivery line; or a percentage of the air present in the fluid delivery line or the probability of the air being in the fluid delivery line.

A cardioplegic agent delivery system comprises a supply reservoir (40) for a cardioplegic agent carrier fluid, a delivery channel from the supply reservoir (40) to an outlet (48), and a pump (50) to flow the carrier liquid in the delivery channel above a minimum driving pressure. The supply reservoir (40) is configured to hold carrier fluid below the minimum driving pressure. The pump (50) is a centrifugal pump configured to receive carrier fluid from the supply reservoir (40) and to flow the carrier fluid to the outlet (48) at a flow rate and above the minimum driving pressure for the delivery of cardioplegic agent. This allows cardioplegia delivery to be managed better.